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BMRN Overview

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$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
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Intellectia

Loading chart...

High
60.850
Open
59.680
VWAP
60.10
Vol
964.89K
Mkt Cap
11.60B
Low
59.510
Amount
57.99M
EV/EBITDA(TTM)
11.18
Total Shares
192.32M
EV
10.64B
EV/OCF(TTM)
12.85
P/S(TTM)
3.64
BioMarin Pharmaceutical Inc. is a global biotechnology company engaged in the development of genetic discovery into medicines that make an impact on the life of each patient. The Company has eight commercial therapies and a clinical and preclinical pipeline. Its commercial products include Vimizim (elosulfase alpha), Naglazyme (galsulfase), Palynziq (pegvaliase-pqpz), Brineura (cerliponase alfa), Aldurazyme (laronidase), Roctavian (valoctocogene roxaparvovec), Kuvan (sapropterin dihydrochloride), and Voxzogo (vosoritide). Vimizim is an enzyme replacement therapy for the treatment of MPS IVA, a lysosomal storage disorder. The Roctavian is an adeno-associated virus (AAV5) vector gene therapy designed to restore factor VIII plasma concentrations in patients with severe hemophilia A. Its key clinical programs include Vosoritide, BMN 333, BMN 390, BMN 351, BMN 349, and INZ-701. Its late-stage enzyme replacement therapy, INZ-701, is being developed for the treatment of ENPP1 deficiency.
Show More

Events Timeline

(ET)
2026-03-12
09:10:00
BioMarin Announces Positive Data from Voxzogo Clinical Trials
select
2026-03-01 (ET)
2026-03-01
11:50:00
BioMarin Receives FDA Approval for Palynziq in Patients 12 and Older
select

News

PRnewswire
9.0
13:55 PMPRnewswire
VOXZOGO Treatment Shows Significant Improvements in Children's Skeletal Growth
  • Early Treatment Impact: New data indicates that children starting VOXZOGO treatment before age 2 experienced an average height increase of 4.7 cm (p=0.0002) after four years, underscoring the critical importance of early intervention for skeletal growth.
  • Proportionality Improvements: Among children treated with VOXZOGO, the upper-to-lower body segment ratio (ULBR) improved by 0.33 (p=0.0005) in the first year and further improved to 0.53 (p<0.0001) by year four, demonstrating the drug's effectiveness in enhancing body proportionality.
  • Global Clinical Evidence: More than 5,000 children across over 50 countries have received VOXZOGO, with Japanese children showing an average height increase of 9.91 cm at 12 months and 15.62 cm at 24 months, further validating the drug's efficacy and safety.
  • Long-Term Safety Studies: BioMarin will present findings on VOXZOGO's long-term safety and growth outcomes at the 2026 ACMG Annual Clinical Genetics Meeting, emphasizing its significant role in children's skeletal development and aiding communication between physicians and families.
Newsfilter
9.0
13:43 PMNewsfilter
VOXZOGO Shows Significant Efficacy in Children
  • Early Treatment Impact: New data indicates that children starting VOXZOGO treatment before age 2 experienced an average height increase of 4.7 cm over four years (p=0.0002), underscoring the significant impact of early intervention on skeletal growth and reinforcing VOXZOGO's status as the only approved treatment.
  • Proportionality Improvement: Among children treated with VOXZOGO, the upper-to-lower body segment ratio (ULBR) improved by 0.33 (p=0.0005) in the first year and reached 0.53 (p<0.0001) by year four, indicating that early treatment enhances not only height but also overall body proportionality, which is crucial for health.
  • Global Evidence Support: More than 5,000 children across over 50 countries have received VOXZOGO, with Japanese children showing an average height increase of 9.91 cm at 12 months and 15.62 cm at 24 months, further validating the efficacy and safety of VOXZOGO.
  • Clinical Research Findings: BioMarin will present these research results at the 2026 American College of Medical Genetics and Genomics Annual Meeting, emphasizing the importance of VOXZOGO in children's skeletal development and facilitating communication between families and healthcare providers.
Benzinga
6.5
03-10Benzinga
BridgeBio's Promising Biotech Pipeline Highlighted by William Blair
  • Unique Market Position: Analyst John Boyle highlights BridgeBio's unique position with the accelerating launch of Attruby and near-term NDA submissions, setting the stage for late-2026/early-2027 launches in the rare genetic disease treatment market.
  • Product Competitive Edge: Market surveys indicate that prescribers view both Attruby and Amvuttra as superior to Pfizer's Tafamidis, which has approximately $6 billion in annual sales, suggesting that BridgeBio's products are gaining traction in clinical applications.
  • Sales Forecast and Risks: The analyst models U.S. sales of Attruby reaching $3.4 billion by 2035, while acknowledging potential generic entry risks in late 2028; however, Attruby's strong TTR stabilization and simple twice-daily dosing could justify premium pricing.
  • Other Market Opportunities: BridgeBio also sees significant market opportunities with other rare disease drugs, particularly infigratinib for achondroplasia and encaleret for autosomal dominant hypocalcemia type 1, with the latter achieving its primary endpoint in the CALIBRATE Phase 3 study in October 2025, indicating strong future prospects.
Yahoo Finance
4.5
03-07Yahoo Finance
BioMarin Pharmaceutical Outlines Strategic Refresh and Market Outlook
  • Strategic Update: BioMarin Pharmaceutical emphasized its strategic refresh at the TD Cowen conference, particularly through the Inozyme deal and the pending Amicus acquisition, aiming to expand enzyme therapy scale across approximately 80 countries, thereby enhancing its competitive position in the rare disease market.
  • Revenue Outlook: Despite anticipating a roughly 3% revenue headwind in 2026 due to the removal of ROCTAVIAN and Kuvan revenue declines, BioMarin expects core enzyme and skeletal businesses to grow at mid-to-high single digits, targeting a 40% operating margin by 2026.
  • Competitive Dynamics: BioMarin anticipates new FDA-approved competition for Voxzogo; however, management believes that patient switching will be gradual due to its five-year market lead and strong patient adherence, which will help maintain market share.
  • Clinical Catalysts: BioMarin is advancing multiple clinical trials, including a Phase 3 study for hypochondroplasia and a pediatric Phase 3 study for BMN 401, which are expected to provide significant growth drivers for the company, particularly in the global rare disease treatment landscape.
NASDAQ.COM
9.0
03-06NASDAQ.COM
FDA Grants Approvals for Multiple New Therapies
  • Hernexeos Approval: On February 26, 2026, the FDA granted accelerated approval to Boehringer Ingelheim's Hernexeos as a first-line treatment for adult patients with HER2-mutant advanced non-small cell lung cancer, representing a significant milestone that could improve patient prognosis and reduce the risk of brain metastases for the 2-4% of NSCLC cases affected.
  • Yuviwel Launch: Ascendis Pharma secured FDA approval on February 27, 2026, for Yuviwel, the first and only therapy providing continuous systemic exposure to C-type natriuretic peptide (CNP) for children aged 2 and older with achondroplasia, which is expected to enhance treatment adherence compared to daily alternatives.
  • Palynziq Indication Expansion: BioMarin received FDA approval on February 27, 2026, to expand Palynziq's indication to include pediatric patients aged 12 and older with phenylketonuria, which is anticipated to further drive sales growth, having generated $433 million in revenue in 2025.
  • Sogroya New Indications: Novo Nordisk obtained FDA approval on February 27, 2026, for Sogroya's expanded indications for various growth disorders, offering a once-weekly growth hormone alternative that is expected to improve treatment adherence and alleviate the burden of daily injections for families.
CNBC
9.0
03-05CNBC
UniQure's Gene Therapy Faces FDA Challenges
  • FDA Study Requirement: The U.S. FDA has mandated that UniQure conduct a placebo-controlled trial to validate the efficacy of its gene therapy for Huntington's disease, despite the company's claims that such a trial is unethical due to the need for prolonged general anesthesia.
  • Clinical Trial Controversy: An FDA official indicated that UniQure's clinical trial data does not meet approval criteria, suggesting that the company may be aware of its earlier trial failures and has not pursued necessary clinical studies.
  • Stock Price Fluctuation: Despite facing challenges from the FDA, UniQure's stock rose over 10% on Thursday, although it has fallen 58% this year, reflecting market concerns regarding the therapy's prospects.
  • Regulatory Tensions: The relationship between UniQure and the FDA is increasingly strained, with the agency facing criticism for recent drug application rejections, and UniQure accusing the FDA of reversing its acceptance standards for the company's clinical trial data.
Wall Street analysts forecast BMRN stock price to rise
19 Analyst Rating
Wall Street analysts forecast BMRN stock price to rise
14 Buy
5 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
60.00
Averages
87.35
High
120.00
Current: 0.000
sliders
Low
60.00
Averages
87.35
High
120.00
BofA
Buy
downgrade
$97 -> $85
AI Analysis
2026-03-11
New
Reason
BofA
Price Target
$97 -> $85
AI Analysis
2026-03-11
New
downgrade
Buy
Reason
BofA lowered the firm's price target on BioMarin to $85 from $97 and keeps a Buy rating on the shares. The firm, which updated its outlook for the pro-forma company ahead of the close of BioMarin's Amicus deal in Q2, says its reduced target largely reflects more conservative assumptions on the Voxzogo-franchise tail.
Barclays
NULL -> Overweight
maintain
$80 -> $105
2026-03-04
Reason
Barclays
Price Target
$80 -> $105
2026-03-04
maintain
NULL -> Overweight
Reason
Barclays raised the firm's price target on BioMarin to $105 from $80 and keeps an Overweight rating on the shares. The firm updated the company's model to include Amicus and the Voxzogo indication expansion. It sees both as key value drivers for the shares.
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for BMRN
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Valuation Metrics

The current forward P/E ratio for BioMarin Pharmaceutical Inc (BMRN.O) is 13.45, compared to its 5-year average forward P/E of 38.52. For a more detailed relative valuation and DCF analysis to assess BioMarin Pharmaceutical Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PE
38.52
Current PE
13.45
Overvalued PE
62.94
Undervalued PE
14.09

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
48.44
Current EV/EBITDA
10.90
Overvalued EV/EBITDA
112.03
Undervalued EV/EBITDA
-15.15

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
6.08
Current PS
3.39
Overvalued PS
7.70
Undervalued PS
4.45

Financials

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Whales Holding BMRN

I
Investor AB (publ)
Holding
BMRN
+59.34%
3M Return
E
Eleva Capital S.A.S.
Holding
BMRN
+18.39%
3M Return
P
PRIMECAP Management Company
Holding
BMRN
+13.64%
3M Return
B
Bluebox Asset Management Uk Ltd.
Holding
BMRN
+6.75%
3M Return
V
Vestal Point Capital, LP
Holding
BMRN
+6.42%
3M Return
S
Sofinnova Investment, Inc.
Holding
BMRN
+4.38%
3M Return

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Frequently Asked Questions

What is BioMarin Pharmaceutical Inc (BMRN) stock price today?

The current price of BMRN is 59.93 USD — it has decreased -0.65

What is BioMarin Pharmaceutical Inc (BMRN)'s business?

BioMarin Pharmaceutical Inc. is a global biotechnology company engaged in the development of genetic discovery into medicines that make an impact on the life of each patient. The Company has eight commercial therapies and a clinical and preclinical pipeline. Its commercial products include Vimizim (elosulfase alpha), Naglazyme (galsulfase), Palynziq (pegvaliase-pqpz), Brineura (cerliponase alfa), Aldurazyme (laronidase), Roctavian (valoctocogene roxaparvovec), Kuvan (sapropterin dihydrochloride), and Voxzogo (vosoritide). Vimizim is an enzyme replacement therapy for the treatment of MPS IVA, a lysosomal storage disorder. The Roctavian is an adeno-associated virus (AAV5) vector gene therapy designed to restore factor VIII plasma concentrations in patients with severe hemophilia A. Its key clinical programs include Vosoritide, BMN 333, BMN 390, BMN 351, BMN 349, and INZ-701. Its late-stage enzyme replacement therapy, INZ-701, is being developed for the treatment of ENPP1 deficiency.

What is the price predicton of BMRN Stock?

Wall Street analysts forecast BMRN stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for BMRN is87.35 USD with a low forecast of 60.00 USD and a high forecast of 120.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is BioMarin Pharmaceutical Inc (BMRN)'s revenue for the last quarter?

BioMarin Pharmaceutical Inc revenue for the last quarter amounts to 874.57M USD, increased 17.03

What is BioMarin Pharmaceutical Inc (BMRN)'s earnings per share (EPS) for the last quarter?

BioMarin Pharmaceutical Inc. EPS for the last quarter amounts to -0.24 USD, decreased -137.50

How many employees does BioMarin Pharmaceutical Inc (BMRN). have?

BioMarin Pharmaceutical Inc (BMRN) has 3221 emplpoyees as of March 12 2026.

What is BioMarin Pharmaceutical Inc (BMRN) market cap?

Today BMRN has the market capitalization of 11.60B USD.